Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045595Generated: October 30, 2026

Cyclopentanecarboxylic acid → HCID 67439957, compound

https://huagongshe.com/reaction/2045595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanecarboxylic acidHCID 18840—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67441230HCID 67441230—
SolventDichloromethaneHCID 6344—
ProductHCID 67439957HCID 6743995790%

Reaction Steps

To an ice-cold mixture of 2-(4-fluoro-3-nitrophenyl)-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate (0.3 mmol, 1.0 eq.), cyclopentanecarboxylic acid (0.46 mmol, 1.5 eq.), N,N-diisopropyl ethylamine (0.6 mmol, 2.0 eq.) in dichloromethane (5 mL) was added a solution of phosphorus oxychloride (0.36 mmol, 1.2 eq.). Then the reaction mixture was stirred at room temperature for 2.5 hours. LC-MS indicated that the starting material was consumed completely. The reaction was quenched by 20 mL water extracted with ethyl acetate (20 mL×2). The combined organic layer was concentrated and the residue was purified by column chromatography (petroleum ether/ethyl acetate=3:1) to afford methyl 2-(3-(cyclopentanecarboxamido)-4-fluorophenyl)-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate as a pale yellow solid; Yield: 90%; MS (ESI+APCI) M+1=425.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586747B2
Source datasetuspto-grants-2013_11
ORD IDord-aa769d0d26b44346b134db95a2d5f0f9
Source noteuspto-grants-2013_11